FIELD: chemistry.
SUBSTANCE: invention relates specifically to compounds with formula (I) and their pharmaceutically acceptable salts that selectively inhibit MCT4 (monocarboxylate transporter 4), pharmaceutical compositions based thereon, their use for obtaining a drug and a method for treating MCT4-mediated cancer.
EFFECT: development of compounds that selectively inhibit MCT4 (monocarboxylate transporter 4). In general formula (I), R1 and R2 are each independently hydrogen or methyl; X is CH2 or O; each ring A and ring B is independently a ring selected from phenyl, pyridinyl, pyrazinyl, pyrimidinyl and pyridazinyl, where each ring A and ring B is independently optionally substituted with one or more substituents selected from C1-3 alkyl and C1 -3 alkoxy; ring C is a 5-9 membered monocyclic or bicyclic saturated heterocycloalkyl optionally containing one or more additional heteroatoms independently selected from O, N and S, where ring C is optionally substituted with one or more substituents selected from C1-3 alkyl optionally substituted with methoxy or hydroxyl; dioxo, C0-2 alkyl-C(O)N(Me)2, C(O)C1-2 alkyl and S(O)2C1-2 alkyl.
23 cl, 5 dwg, 3 tbl, 87 ex
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Authors
Dates
2023-03-30—Published
2019-05-10—Filed